tert-butyl 6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate
tert-butyl 6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate
CAS: 230301-11-8
Molecular Formula: C11H17N3O2
tert-butyl 6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate - Names and Identifiers
tert-butyl 6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate - Physico-chemical Properties
| Molecular Formula | C11H17N3O2 |
| Molar Mass | 223.27 |
| Density | 1.200±0.06 g/cm3(Predicted) |
| Boling Point | 388.0±42.0 °C(Predicted) |
| pKa | 14.81±0.20(Predicted) |
| Storage Condition | 2-8°C |
tert-butyl 6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate - Introduction
tert-butyl [4,3-c]pyridine-5(4H)-carboxylate is an organic compound with the chemical formula C14H20N2O2. It is a white solid.
The main use of this compound is as a protecting group in organic synthesis. It can be achieved by protecting the hydrogen atom at the C- 5 position of the pyrazolo [4,3-c] pyridine in order to carry out the chemical reaction without affecting the reaction at other positions. After completion of the reaction, the 5-BOC group can be easily removed by appropriate conditions.
tert-butyl 6, [4,3-c]pyridine-5(4H)-carboxylate is usually prepared by using pyrazole [4,3-c]pyridine as raw material, after protection reaction and esterification reaction. Specific synthetic steps and conditions may vary depending on laboratory conditions.
Regarding safety information, this compound is generally stable and relatively safe under regular conditions. However, like most compounds, it may have irritating effects on the skin, eyes and respiratory system. Wear protective gloves, face shield and goggles during use and operation, and ensure that the operation is carried out in a well-ventilated place. If exposed or inhaled, rinse immediately with plenty of water and seek medical help. It is also important that this compound is stored and handled correctly, and that the relevant safety procedures be followed.
The main use of this compound is as a protecting group in organic synthesis. It can be achieved by protecting the hydrogen atom at the C- 5 position of the pyrazolo [4,3-c] pyridine in order to carry out the chemical reaction without affecting the reaction at other positions. After completion of the reaction, the 5-BOC group can be easily removed by appropriate conditions.
tert-butyl 6, [4,3-c]pyridine-5(4H)-carboxylate is usually prepared by using pyrazole [4,3-c]pyridine as raw material, after protection reaction and esterification reaction. Specific synthetic steps and conditions may vary depending on laboratory conditions.
Regarding safety information, this compound is generally stable and relatively safe under regular conditions. However, like most compounds, it may have irritating effects on the skin, eyes and respiratory system. Wear protective gloves, face shield and goggles during use and operation, and ensure that the operation is carried out in a well-ventilated place. If exposed or inhaled, rinse immediately with plenty of water and seek medical help. It is also important that this compound is stored and handled correctly, and that the relevant safety procedures be followed.
Last Update：2024-04-10 22:29:15
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Product Name: tert-butyl 6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxylate Visit Supplier Webpage Request for quotation
CAS: 230301-11-8
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Mobile: 18021002903
QQ: 3008007409
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CAS: 230301-11-8
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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